Estimating the Value of Aztreonam-Avibactam in Treating Metallo-beta-Lactamase-Producing Enterobacterales Infections in Spain Using the STEDI AMR Value Framework.

IF 5.3 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2025-09-01 Epub Date: 2025-07-28 DOI:10.1007/s40121-025-01202-6
Ricard Ferrer, Sonia Luque, Luis Martínez-Martínez, Alfonso de Lossada, Marta Maroto-Diaz, Carlota Moya-Alarcón, Maria Carmen de Ceano-Vivas, Yolanda Moreno, James Dennis, Silviya Nikolova, Evangelos Zormpas, Edward Broughton, Maria Gheorghe
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引用次数: 0

Abstract

Introduction: Treatments for serious infections caused by multidrug-resistant gram-negative bacteria, including metallo-β-lactamase-producing Enterobacterales (MBL-EB), are limited and aztreonam with avibactam (ATM-AVI) is the first β-lactam/β-lactamase inhibitor combination active against MBL-EB approved in Europe and approved for reimbursement by the Spanish National Health System (NHS). This study aims to estimate the value of adding ATM-AVI as a new first-line treatment into the current strategy (ATM-AVI → cefiderocol → colistin + meropenem) in patients with hospital-acquired/ventilator-associated pneumonia (HAP/VAP) and complicated intra-abdominal infections (cIAI), caused by MBL-EB from the Spanish NHS perspective.

Methods: A dynamic disease transmission model was developed to assess the value of ATM-AVI considering the transmission, diversity and enablement components of the value framework for antibiotics, called STEDI (spectrum, transmission, enablement, diversity, insurance). Transmission and diversity value were described by estimating direct population-level impact on treatment outcomes and resistance development. Enablement value was estimated by linking population-level improvements in antimicrobial effectiveness into improved prophylactic effectiveness. Inputs for efficacy, resistance, adverse events, and costs were sourced from the REVISIT study, literature and expert opinion. A 10-year infection transmission horizon was used; quality-adjusted life years (QALYs) were estimated over a lifetime and valued using a willingness-to-pay (WTP) threshold of €25,000/QALY gained to calculate the net monetary benefit (NMB). Costs and benefits were discounted at a rate of 3%.

Results: Over 10 years, the intervention strategy introducing ATM-AVI was dominant, leading to a 2.96% proportional reduction in resistance, 19,533 fewer infections and 4662 lives saved (47,319 QALYs gained) and a cost saving of €40.5 million. The NMB was €1.22 billion.

Conclusions: In Spain, ATM-AVI is a highly cost-effective and urgently needed treatment option for patients with MBL-EB including HAP/VAP and cIAI infections. Using the novel STEDI framework unlocks the considerable value of a new antibiotic which is essential to support incentives for the development of new antimicrobials.

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利用STEDI AMR值框架估计氨曲南-阿维巴坦治疗西班牙产金属-内酰胺酶肠杆菌感染的价值。
介绍:对多重耐药革兰氏阴性菌(包括产生金属β-内酰胺酶的肠杆菌(MBL-EB))引起的严重感染的治疗是有限的,aztreonam与avibactam (ATM-AVI)是欧洲批准的第一个抗MBL-EB的β-内酰胺/β-内酰胺酶抑制剂组合,并被西班牙国家卫生系统(NHS)批准报销。本研究旨在从西班牙NHS的角度评估将ATM-AVI作为一种新的一线治疗方法加入到目前的治疗策略(ATM-AVI→头孢地罗→粘菌素+美罗培钠)中,对由MBL-EB引起的医院获得性/呼吸机相关性肺炎(HAP/VAP)和并发腹腔内感染(cIAI)患者的价值。方法:建立一个动态疾病传播模型,考虑抗生素价值框架STEDI(频谱、传播、使能、多样性、保险)的传播、多样性和使能成分,评估ATM-AVI的价值。通过估计对治疗结果和耐药性发展的直接人群水平影响来描述传播和多样性价值。通过将人群水平上抗菌效果的改善与预防效果的改善联系起来,估计了实现值。关于疗效、耐药性、不良事件和成本的输入来自于重访研究、文献和专家意见。采用10年感染传播水平;质量调整生命年(QALYs)在一生中进行估计,并使用25,000欧元/QALY的支付意愿(WTP)阈值来计算净货币效益(NMB)。成本和收益按3%折现。结果:10年间,引入ATM-AVI的干预策略占主导地位,使耐药比例降低2.96%,减少感染19,533例,挽救生命4662例(获得47,319个QALYs),节省成本4050万欧元。NMB为12.2亿欧元。结论:在西班牙,对于包括HAP/VAP和cIAI感染在内的MBL-EB患者,ATM-AVI是一种高成本效益和迫切需要的治疗选择。使用新的STEDI框架释放了一种新抗生素的巨大价值,这对于支持开发新的抗微生物药物的激励措施至关重要。
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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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